| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43527159-43527521 | Common:6; Rare:107; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575451-43575746 | Common:2; Rare:89 | ||||
| chr19:43596002-43596500 | Common:4; Rare:154 | ||||
| chr19:43668692-43669040 | Common:3; Rare:71 | ||||
| chr19:43670151-43670365 | Common:2; Rare:51 | ||||
| chr19:43735029-43735139 | Common:2; Rare:22 | ||||
| chr19:43754663-43754741 | Common:1; Rare:27 | ||||
| chr19:43754773-43755127 | Common:3; Rare:125 | ||||
| chr19:43901749-43901875 | Common:1; Rare:26 | ||||
| chr19:44002819-44003010 | Common:4; Rare:50 | ||||
| chr19:44060542-44060792 | Rare:56 | ||||
| chr19:44072013-44072176 | Common:1; Rare:38 | ||||
| chr19:44094203-44094435 | Common:1; Rare:61 | ||||
| chr19:44113217-44113470 | Common:3; Rare:53 | ||||
| chr19:44141473-44141647 | Common:2; Rare:24 |